Jiddane M, Nicoli F, Diaz P, Bergvall U, Vincentelli F, Hassoun J, Salamon G
J Neurosurg. 1986 Nov;65(5):592-9. doi: 10.3171/jns.1986.65.5.0592.
Although primary malignant lymphoma is a rare entity in the gamut of intracranial tumors, it is more frequently seen than the secondary intracranial spread of a primary extracranial lymphoma. In general, the occurrence of lymphomas seems to be provoked by immunosuppression, as with medication (predominantly after transplantation) or with immunodepressive disease such as acquired immunodeficiency syndrome (AIDS). The usual age of onset of this disease is 55 to 65 years; and the male:female patient distribution is roughly 2:1. Characteristically, computerized tomography (CT) scans of lymphomas show a mass which is often large with regular contours, moderate mass effect, and hyper- or isodensity with marked and often homogeneous enhancement. In the series of 30 patients reported, the locations of lesions, in order of decreasing frequency, were the frontocallosal and temporal regions, the basal ganglia, and the cerebellum. Multiple lesions were present in 15% of these cases (20% to 40% in the literature). The following features should raise the suspicion of intracranial lymphoma: mirror lesions of the basal ganglia, bilateral subependymal infiltration, and leptomeningeal involvement contiguous with an intracerebral mass. According to the literature, the angiographic finding typical of lymphoma is an avascular tumor. A blush or vascular encasement of the mass seems to be rare, and the present series was in accordance with other reports in this respect. Differential diagnostic consideration should include meningioma, glioblastoma, metastatic disease, and focal infectious lesions such as toxoplasmosis or multifocal progressive leukoencephalitis, particularly in immunodepressed subjects. Diagnosing lymphoma from CT scans offers the alternative of substituting stereotaxic biopsy and neuropathological diagnosis for the more aggressive open surgical approach, since radiation therapy and possibly chemotherapy usually prove to be the treatment of choice.
虽然原发性恶性淋巴瘤在颅内肿瘤中是一种罕见的类型,但它比原发性颅外淋巴瘤的继发性颅内扩散更为常见。一般来说,淋巴瘤的发生似乎是由免疫抑制引发的,如药物治疗(主要是移植后)或免疫抑制性疾病,如获得性免疫缺陷综合征(艾滋病)。这种疾病的通常发病年龄为55至65岁;男女患者分布比例约为2:1。典型的是,淋巴瘤的计算机断层扫描(CT)显示一个肿块,通常较大,轮廓规则,有中度占位效应,密度高于或等于周围组织,并有明显且通常均匀的强化。在所报告的30例患者系列中,病变部位按频率递减顺序依次为额胼胝体和颞叶区域、基底节和小脑。这些病例中有15%存在多发病变(文献报道为20%至40%)。以下特征应引起对颅内淋巴瘤的怀疑:基底节的镜像病变、双侧室管膜下浸润以及与脑内肿块相邻的软脑膜受累。根据文献,淋巴瘤典型的血管造影表现是无血管肿瘤。肿块出现造影剂充盈或血管包绕似乎很少见,本系列在这方面与其他报告一致。鉴别诊断应考虑脑膜瘤、胶质母细胞瘤、转移性疾病以及局灶性感染性病变,如弓形虫病或多灶性进行性白质脑病,特别是在免疫抑制患者中。通过CT扫描诊断淋巴瘤提供了一种替代方法,即采用立体定向活检和神经病理学诊断来替代更激进的开放手术方法,因为放射治疗以及可能的化疗通常被证明是首选治疗方法。